Canonical Allele Identifier: PA099523
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 7351
ClinVar RCV Id: RCV000007776 RCV000199127 RCV003904817 RCV003488330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Pro130Ser
CA254151
NM_001099679.2:c.388C>T